Decreasing in the incidence of pain component while injection during unconsciouness of the perso
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2021/04/032881
- Lead Sponsor
- Dr Aravind
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.ASA 1 and 2 patients
2.Age more than 18 years
3.Patients undergoing general anaesthesia
4.Patients acceptance
5.Patients with Propofol as induction agent
Exclusion Criteria
1.Patients allergic to Propofol and Ketamine
2.Patients allergic to egg
3.Patietns with cardiovascular, neurologica and respiratory diseases
4.ASA 3 and 4
5.Emergency Surgeries
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary outcome of this study is to compare the effect of low dose ketamine and 2% lignocaine pretreatment in preventing pain on propofol injection (POPI ) with verbal rating scale ( 0-3 ) and its haemodynamic responses. <br/ ><br> <br/ ><br>Timepoint: The primary outcome of this study is to compare the effect of low dose ketamine and 2% lignocaine pretreatment in preventing pain on propofol injection (POPI ) with verbal rating scale ( 0-3 ) and its haemodynamic responses. <br/ ><br>Assessed during injection, o minute, 1,2,3 and 5 minutes and the outcome is predicted.
- Secondary Outcome Measures
Name Time Method Haemodynamic parameters like heart rate, systolic blood pressure, diastolic blood pressure, mean arterial pressure and oxygen saturation monitoredTimepoint: every one minute till 10 minutes